BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

359 related articles for article (PubMed ID: 16326079)

  • 1. FGF signaling is necessary for establishing gut tube domains along the anterior-posterior axis in vivo.
    Dessimoz J; Opoka R; Kordich JJ; Grapin-Botton A; Wells JM
    Mech Dev; 2006 Jan; 123(1):42-55. PubMed ID: 16326079
    [TBL] [Abstract][Full Text] [Related]  

  • 2. FGF2 specifies hESC-derived definitive endoderm into foregut/midgut cell lineages in a concentration-dependent manner.
    Ameri J; Ståhlberg A; Pedersen J; Johansson JK; Johannesson MM; Artner I; Semb H
    Stem Cells; 2010 Jan; 28(1):45-56. PubMed ID: 19890880
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of molecular markers that are expressed in discrete anterior-posterior domains of the endoderm from the gastrula stage to mid-gestation.
    Moore-Scott BA; Opoka R; Lin SC; Kordich JJ; Wells JM
    Dev Dyn; 2007 Jul; 236(7):1997-2003. PubMed ID: 17576135
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Impact of node ablation on the morphogenesis of the body axis and the lateral asymmetry of the mouse embryo during early organogenesis.
    Davidson BP; Kinder SJ; Steiner K; Schoenwolf GC; Tam PP
    Dev Biol; 1999 Jul; 211(1):11-26. PubMed ID: 10373301
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Regional specification of the endoderm in the early chick embryo.
    Kimura W; Yasugi S; Fukuda K
    Dev Growth Differ; 2007 Jun; 49(5):365-72. PubMed ID: 17428263
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Regulation of Hex gene expression and initial stages of avian hepatogenesis by Bmp and Fgf signaling.
    Zhang W; Yatskievych TA; Baker RK; Antin PB
    Dev Biol; 2004 Apr; 268(2):312-26. PubMed ID: 15063170
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Sequential allocation and global pattern of movement of the definitive endoderm in the mouse embryo during gastrulation.
    Tam PP; Khoo PL; Lewis SL; Bildsoe H; Wong N; Tsang TE; Gad JM; Robb L
    Development; 2007 Jan; 134(2):251-60. PubMed ID: 17151016
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Retinoic acid signaling organizes endodermal organ specification along the entire antero-posterior axis.
    Bayha E; Jørgensen MC; Serup P; Grapin-Botton A
    PLoS One; 2009 Jun; 4(6):e5845. PubMed ID: 19516907
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cell fate decisions within the mouse organizer are governed by graded Nodal signals.
    Vincent SD; Dunn NR; Hayashi S; Norris DP; Robertson EJ
    Genes Dev; 2003 Jul; 17(13):1646-62. PubMed ID: 12842913
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Different thresholds of fibroblast growth factors pattern the ventral foregut into liver and lung.
    Serls AE; Doherty S; Parvatiyar P; Wells JM; Deutsch GH
    Development; 2005 Jan; 132(1):35-47. PubMed ID: 15576401
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Foxh1 and Foxa2 are not required for formation of the midgut and hindgut definitive endoderm.
    McKnight KD; Hou J; Hoodless PA
    Dev Biol; 2010 Jan; 337(2):471-81. PubMed ID: 19896480
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two ParaHox genes, SpLox and SpCdx, interact to partition the posterior endoderm in the formation of a functional gut.
    Cole AG; Rizzo F; Martinez P; Fernandez-Serra M; Arnone MI
    Development; 2009 Feb; 136(4):541-9. PubMed ID: 19144720
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Retinoic acid signaling targets Hox genes during the amphioxus gastrula stage: insights into early anterior-posterior patterning of the chordate body plan.
    Koop D; Holland ND; Sémon M; Alvarez S; de Lera AR; Laudet V; Holland LZ; Schubert M
    Dev Biol; 2010 Feb; 338(1):98-106. PubMed ID: 19914237
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Wnt co-receptors Lrp5 and Lrp6 are essential for gastrulation in mice.
    Kelly OG; Pinson KI; Skarnes WC
    Development; 2004 Jun; 131(12):2803-15. PubMed ID: 15142971
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inhibition of FGF signaling causes expansion of the endoderm in Xenopus.
    Cha SW; Hwang YS; Chae JP; Lee SY; Lee HS; Daar I; Park MJ; Kim J
    Biochem Biophys Res Commun; 2004 Feb; 315(1):100-6. PubMed ID: 15013431
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The pitx2 homeobox protein is required early for endoderm formation and nodal signaling.
    Faucourt M; Houliston E; Besnardeau L; Kimelman D; Lepage T
    Dev Biol; 2001 Jan; 229(2):287-306. PubMed ID: 11203696
    [TBL] [Abstract][Full Text] [Related]  

  • 17. FGF is required for posterior neural patterning but not for neural induction.
    Holowacz T; Sokol S
    Dev Biol; 1999 Jan; 205(2):296-308. PubMed ID: 9917365
    [TBL] [Abstract][Full Text] [Related]  

  • 18. FoxD5 mediates anterior-posterior polarity through upstream modulator Fgf signaling during zebrafish somitogenesis.
    Lee HC; Tseng WA; Lo FY; Liu TM; Tsai HJ
    Dev Biol; 2009 Dec; 336(2):232-45. PubMed ID: 19818746
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Control of early anterior-posterior patterning in the mouse embryo by TGF-beta signalling.
    Robertson EJ; Norris DP; Brennan J; Bikoff EK
    Philos Trans R Soc Lond B Biol Sci; 2003 Aug; 358(1436):1351-7; discussion 1357. PubMed ID: 14511481
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Subdividing the embryo: a role for Notch signaling during germ layer patterning in Xenopus laevis.
    Contakos SP; Gaydos CM; Pfeil EC; McLaughlin KA
    Dev Biol; 2005 Dec; 288(1):294-307. PubMed ID: 16289076
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.